Sterilance soft twist lancet

GUDID 06945630108709

Sterilance soft twist lancet,30G,100Lancets/box

SteriLance Medical (Suzhou) Inc.

Blood lancet, single-use Blood lancet, single-use Blood lancet, single-use Blood lancet, single-use Blood lancet, single-use Blood lancet, single-use Blood lancet, single-use Blood lancet, single-use Blood lancet, single-use Blood lancet, single-use Blood lancet, single-use Blood lancet, single-use Blood lancet, single-use Blood lancet, single-use Blood lancet, single-use
Primary Device ID06945630108709
NIH Device Record Key361e664a-dd29-4334-a438-06395d6482a6
Commercial Distribution StatusIn Commercial Distribution
Brand NameSterilance soft twist lancet
Version Model Number01-0130
Company DUNS421141183
Company NameSteriLance Medical (Suzhou) Inc.
Device Count100
DM Exemptfalse
Pre-market Exempttrue
MRI Safety StatusLabeling does not contain MRI Safety Information
Human Cell/Tissue Productfalse
Device Kitfalse
Device Combination Productfalse
Single Usetrue
Lot Batchtrue
Serial Numberfalse
Manufacturing Datefalse
Expiration Datetrue
Donation Id Numberfalse
Contains Natural Rubber Latexfalse
Labeled No Natural Rubber Latexfalse
RX Perscriptionfalse
OTC Over-The-Countertrue

Device Identifiers

Device Issuing AgencyDevice ID
GS106945630108709 [Unit of Use]
GS116945630108706 [Primary]

FDA Product Code

FMKLancet, Blood

Sterilization

Steralize Prior To Usefalse
Device Is Steriletrue

Device Entry Metadata

Public Version StatusNew
Device Record StatusPublished
Public Version Number1
Public Version Date2020-11-05
Device Publish Date2020-10-28

On-Brand Devices [Sterilance soft twist lancet]

06945630108709Sterilance soft twist lancet,30G,100Lancets/box
06945630108747Sterilance soft twist lancet,33G,100Lancets/box

© 2024 FDA.report
This site is not affiliated with or endorsed by the FDA.